Yeastract
YEASTRACT+ INESC-ID IST IBB
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Regulation Reference(s)

The Yeastract team, is actively curating each regulation evidence code, association type and environmental condition.
Transcription
Factor
Target
ORF/Genes
References Evidence
Code
Evidence
Experiment
Association
Type
Strain Environmental
Group
Environmental
Condition
Log2FC
Ume6p YBR072W PubMed external link Williams RM et al., Proceedings of the National Academy of Sciences of the United States of America, 2002 Oct 15;99(21):13431-6Williams RM et al., Proceedings of the National Academy of Sciences of the United States of America, 2002 Oct 15;99(21):13431-6 Indirect Microarray analysis - wt vs TF mutant Negative SK1 Carbon source quality/availability Cells grown in YPAcetate medium to late log phase N/A
Indirect Microarray analysis - wt vs TF mutant Negative W303 Unstressed log-phase growth (control) Cells grown in YPD medium to late log phase N/A
PubMed external link Lardenois A et al., Molecular genetics and genomics : MGG, 2015 Oct;290(5):2031-46Lardenois A et al., Molecular genetics and genomics : MGG, 2015 Oct;290(5):2031-46 Indirect Microarray analysis - WT vs TF Deletion Negative SK1 Carbon source quality/availability Grown in rich media with acetate (YPA) under standard conditions. Transcription factor gene deletion. -2.339553
PubMed external link van Heusden GPH, Genomics, 2023 Sep;115(5):110672van Heusden GPH, Genomics, 2023 Sep;115(5):110672 Indirect RNA-seq analysis - WT vs TF Deletion Negative BY4741 Ion/metal/phosphate/sulfur/vitamin availability Grown overnight at 30 °C in phosphate-free YNB medium supplemented with 7.2 mM potassium phosphate (pH 5.8), 20 mg/L histidine, leucine, methionine, and uracil, and 50 mM KCl, then used to inoculate 50 mL cultures at OD620 = 0.1 and grown at 30 °C, 180 rpm to OD620 = 0.5. Transcription factor gene deletion. -1.12320455089806
PubMed external link Harris A et al., Genetics, 2023 Oct 4;225(2):Harris A et al., Genetics, 2023 Oct 4;225(2): Indirect RNA-seq analysis - WT vs TF Deletion Positive SK1 Unstressed log-phase growth (control) Mitotic, 30min: Cells were in mitotic, log-phase growth. They were grown in YPD (1% yeast extract, 2% peptone, 2% dextrose, 22.4 mg/L uracil, 80 mg/L tryptophan) for ~24 h to saturation, then back-diluted into fresh YPD to OD600 = 0.2 and grown ~3 h to log phase (OD600 ≥ 0.5). Once in log phase, β-estradiol (40 nM) was added, followed 30 min later by auxin (200 µM) at t=0min. Sampled at 30 min. 0.741346
Indirect RNA-seq analysis - WT vs TF Under-expression Negative SK1 Cell cycle/morphology Meiotic 0.5h: Cells were transitioning from premeiotic starvation into meiosis. They were grown in YPD for ~24 h to saturation, then inoculated into BYTA (1% yeast extract, 2% bacto tryptone, 1% potassium acetate, 50 mM potassium phthalate) at OD600 = 0.25 and grown 16–18 h at 30 °C to OD600 ≥ 5. Cells were then pelleted, washed with sterile water, and resuspended in SPM (2% KOAc, 0.02% raffinose, amino acid supplements, pH 7) at OD600 = 1.85, shaken at 30 °C and 275 rpm. At 0.5 h in SPM, β-estradiol (5 nM) and auxin (200 µM) were added simultaneously, followed by CuSO4 (50 µM) at 2 h to trigger IME1/4 expression and meiotic entry. Sampled at 0.5 h. -1.018074
Indirect RNA-seq analysis - WT vs TF Under-expression Negative SK1 Unstressed log-phase growth (control) Mitotic, 15min: Cells were in mitotic, log-phase growth. They were grown in YPD (1% yeast extract, 2% peptone, 2% dextrose, 22.4 mg/L uracil, 80 mg/L tryptophan) for ~24 h to saturation, then back-diluted into fresh YPD to OD600 = 0.2 and grown ~3 h to log phase (OD600 ≥ 0.5). Once in log phase, β-estradiol (40 nM) was added, followed 30 min later by auxin (200 µM) at t=0min. Sampled at 15 min. -0.4033
Indirect RNA-seq analysis - WT vs TF Under-expression Negative SK1 Cell cycle/morphology Meiotic 2.5h: Cells were transitioning from premeiotic starvation into meiosis. They were grown in YPD for ~24 h to saturation, then inoculated into BYTA (1% yeast extract, 2% bacto tryptone, 1% potassium acetate, 50 mM potassium phthalate) at OD600 = 0.25 and grown 16–18 h at 30 °C to OD600 ≥ 5. Cells were then pelleted, washed with sterile water, and resuspended in SPM (2% KOAc, 0.02% raffinose, amino acid supplements, pH 7) at OD600 = 1.85, shaken at 30 °C and 275 rpm. At 0.5 h in SPM, β-estradiol (5 nM) and auxin (200 µM) were added simultaneously, followed by CuSO4 (50 µM) at 2 h to trigger IME1/4 expression and meiotic entry. Sampled at 2.5 h. -1.864312